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Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor

Author

Listed:
  • Li-Hua Zhao

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Jingyu Lin

    (Shandong University)

  • Su-Yu Ji

    (Zhejiang University School of Medicine)

  • X. Edward Zhou

    (Van Andel Research Institute)

  • Chunyou Mao

    (Zhejiang University School of Medicine)

  • Dan-Dan Shen

    (Zhejiang University School of Medicine)

  • Xinheng He

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Peng Xiao

    (Shandong University)

  • Jinpeng Sun

    (Shandong University)

  • Karsten Melcher

    (Van Andel Research Institute)

  • Yan Zhang

    (Zhejiang University School of Medicine
    Zhejiang University Medical Center
    Zhejiang University School of Medicine
    Zhejiang Provincial Key Laboratory of Immunity and Inflammatory diseases)

  • Xiao Yu

    (Shandong University)

  • H. Eric Xu

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

Abstract

The ability to couple with multiple G protein subtypes, such as Gs, Gi/o, or Gq/11, by a given G protein-coupled receptor (GPCR) is critical for many physiological processes. Over the past few years, the cryo-EM structures for all 15 members of the medically important class B GPCRs, all in complex with Gs protein, have been determined. However, no structure of class B GPCRs with Gq/11 has been solved to date, limiting our understanding of the precise mechanisms of G protein coupling selectivity. Here we report the structures of corticotropin releasing factor receptor 2 (CRF2R) bound to Urocortin 1 (UCN1), coupled with different classes of heterotrimeric G proteins, G11 and Go. We compare these structures with the structure of CRF2R in complex with Gs to uncover the structural differences that determine the selective coupling of G protein subtypes by CRF2R. These results provide important insights into the structural basis for the ability of CRF2R to couple with multiple G protein subtypes.

Suggested Citation

  • Li-Hua Zhao & Jingyu Lin & Su-Yu Ji & X. Edward Zhou & Chunyou Mao & Dan-Dan Shen & Xinheng He & Peng Xiao & Jinpeng Sun & Karsten Melcher & Yan Zhang & Xiao Yu & H. Eric Xu, 2022. "Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-33851-3
    DOI: 10.1038/s41467-022-33851-3
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    References listed on IDEAS

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    1. Javier García-Nafría & Rony Nehmé & Patricia C. Edwards & Christopher G. Tate, 2018. "Cryo-EM structure of the serotonin 5-HT1B receptor coupled to heterotrimeric Go," Nature, Nature, vol. 558(7711), pages 620-623, June.
    2. Fulai Zhou & Huibing Zhang & Zhaotong Cong & Li-Hua Zhao & Qingtong Zhou & Chunyou Mao & Xi Cheng & Dan-Dan Shen & Xiaoqing Cai & Cheng Ma & Yuzhe Wang & Antao Dai & Yan Zhou & Wen Sun & Fenghui Zhao , 2020. "Structural basis for activation of the growth hormone-releasing hormone receptor," Nature Communications, Nature, vol. 11(1), pages 1-10, December.
    3. Yi-Lynn Liang & Maryam Khoshouei & Mazdak Radjainia & Yan Zhang & Alisa Glukhova & Jeffrey Tarrasch & David M. Thal & Sebastian G. B. Furness & George Christopoulos & Thomas Coudrat & Radostin Danev &, 2017. "Phase-plate cryo-EM structure of a class B GPCR–G-protein complex," Nature, Nature, vol. 546(7656), pages 118-123, June.
    4. Fan Yang & Lulu Guo & Yu Li & Guopeng Wang & Jia Wang & Chao Zhang & Guo-Xing Fang & Xu Chen & Lei Liu & Xu Yan & Qun Liu & Changxiu Qu & Yunfei Xu & Peng Xiao & Zhongliang Zhu & Zijian Li & Jiuyao Zh, 2021. "Structure, function and pharmacology of human itch receptor complexes," Nature, Nature, vol. 600(7887), pages 164-169, December.
    5. Jia Duan & Dan-dan Shen & X. Edward Zhou & Peng Bi & Qiu-feng Liu & Yang-xia Tan & You-wen Zhuang & Hui-bing Zhang & Pei-yu Xu & Si-Jie Huang & Shan-shan Ma & Xin-heng He & Karsten Melcher & Yan Zhang, 2020. "Cryo-EM structure of an activated VIP1 receptor-G protein complex revealed by a NanoBiT tethering strategy," Nature Communications, Nature, vol. 11(1), pages 1-10, December.
    6. Shoji Maeda & Antoine Koehl & Hugues Matile & Hongli Hu & Daniel Hilger & Gebhard F. X. Schertler & Aashish Manglik & Georgios Skiniotis & Roger J. P. Dawson & Brian K. Kobilka, 2018. "Development of an antibody fragment that stabilizes GPCR/G-protein complexes," Nature Communications, Nature, vol. 9(1), pages 1-9, December.
    7. Tilman Flock & Alexander S. Hauser & Nadia Lund & David E. Gloriam & Santhanam Balaji & M. Madan Babu, 2017. "Selectivity determinants of GPCR–G-protein binding," Nature, Nature, vol. 545(7654), pages 317-322, May.
    8. Yi-Lynn Liang & Maryam Khoshouei & Alisa Glukhova & Sebastian G. B. Furness & Peishen Zhao & Lachlan Clydesdale & Cassandra Koole & Tin T. Truong & David M. Thal & Saifei Lei & Mazdak Radjainia & Rado, 2018. "Phase-plate cryo-EM structure of a biased agonist-bound human GLP-1 receptor–Gs complex," Nature, Nature, vol. 555(7694), pages 121-125, March.
    9. Yi-Lynn Liang & Maryam Khoshouei & Giuseppe Deganutti & Alisa Glukhova & Cassandra Koole & Thomas S. Peat & Mazdak Radjainia & Jürgen M. Plitzko & Wolfgang Baumeister & Laurence J. Miller & Deborah L., 2018. "Cryo-EM structure of the active, Gs-protein complexed, human CGRP receptor," Nature, Nature, vol. 561(7724), pages 492-497, September.
    10. Yan Zhang & Bingfa Sun & Dan Feng & Hongli Hu & Matthew Chu & Qianhui Qu & Jeffrey T. Tarrasch & Shane Li & Tong Sun Kobilka & Brian K. Kobilka & Georgios Skiniotis, 2017. "Cryo-EM structure of the activated GLP-1 receptor in complex with a G protein," Nature, Nature, vol. 546(7657), pages 248-253, June.
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